Variant information


Systematic Name c.119_120delAG
Protein name p.Glu40fs
Mutation type frameshift insertion or deletion
Domain N-term
Pathogenicity Mutation associated with disease

Proband information


Source of DNA blood
Detection direct
Extent all exons
Number of chromosomes checked
Carrier status checked Yes
Carrier result de novo
Other mutations NK
X-inactivation results
X-inactivation relatives
Gender Female
Sporadic/Familial sporadic
Phenotype-class Rett syndrome-not certain
Reference MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome:Li, M.-R., Pan, H., Bao, X.-H., Zhang, Y.-Z., Wu, X.-R.:Journal of Human Genetics: 17089071

Matching entries in the proband database


No: Systematic Name Protein name Mutation type Domain Pathogenicity Gender Phenotype Proband id References
1 c.119_120delAG p.Glu40fs frameshift insertion or deletion N-term Mutation associated with disease Female Rett syndrome-not certain 3596 MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome:Li, M.-R., Pan, H., Bao, X.-H., Zhang, Y.-Z., Wu, X.-R.:Journal of Human Genetics: 17089071
2 c.119_120delAG p.Glu40fs frameshift insertion or deletion N-term Mutation associated with disease Male Not Rett synd. 3869 A novel MECP2 mutation in a boy with neonatal encephalopathy and facial dysmorphism:Julich, K., Horn, D., Burfeind, P., Erler, T., Auber, B.:J Pediatr: 19559301